BR9712200A - Method for producing glycol - Google Patents
Method for producing glycolInfo
- Publication number
- BR9712200A BR9712200A BR9712200-9A BR9712200A BR9712200A BR 9712200 A BR9712200 A BR 9712200A BR 9712200 A BR9712200 A BR 9712200A BR 9712200 A BR9712200 A BR 9712200A
- Authority
- BR
- Brazil
- Prior art keywords
- glycol
- hydroxyl compound
- reactor
- epoxide
- compound
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/09—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
- C07C29/10—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes
- C07C29/103—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes of cyclic ethers
- C07C29/106—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes of cyclic ethers of oxiranes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/09—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
- C07C29/10—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Epoxy Compounds (AREA)
Abstract
This invention relates to a method for producing glycols. Such a method is particularly useful for preparing ethylene glycol from ethylene oxide and water. The method of this invention is a synergistic combination of the process of evaporation, absorption, and reaction, combined to enhance reactions of yields for reactions of epoxides with compounds containing hydroxy functional groups. Such method comprises making glycol in an evaporation column reactor as follows: (a) feeding a hydroxy compound into the reactor; (b) feeding an epoxide into the reactor such that the epoxide compound is contacted with hydroxyl compound in a reaction zone under conditions such that substantially all of the epoxide reacts to form a product comprising a glycol which is dissolved in liquid hydroxyl compound; (c) removing the mixture of liquid hydroxyl compound and dissolved glycol away from the reaction zone; and (d) heating the mixture of liquid hydroxyl compound and dissolved glycol such that at least some of the hydroxyl compound is evaporated away from the glycol; and (e) condensing and refluxing the evaporated hydroxyl compound and combining it with the hydroxyl compound of Step (a). In one aspect of the invention, the epoxide feed described in Step (b) enter the reactor through at least two distinct ports within the reactor. In another aspect of this invention, the method is synergistically conducted in at least two sequential evaporation columns which together form a multiple effect evaporation column reactor.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US2665996P | 1996-10-04 | 1996-10-04 | |
PCT/US1997/017936 WO1998014419A1 (en) | 1996-10-04 | 1997-10-03 | A method for producing glycols |
Publications (1)
Publication Number | Publication Date |
---|---|
BR9712200A true BR9712200A (en) | 2002-07-16 |
Family
ID=21833100
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR9712200-9A BR9712200A (en) | 1996-10-04 | 1997-10-03 | Method for producing glycol |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP0929503B1 (en) |
JP (1) | JP2001501624A (en) |
KR (1) | KR20000048902A (en) |
CN (1) | CN1100742C (en) |
AT (1) | ATE207050T1 (en) |
AU (1) | AU731453B2 (en) |
BR (1) | BR9712200A (en) |
CA (1) | CA2268158A1 (en) |
DE (1) | DE69707487T2 (en) |
ES (1) | ES2165589T3 (en) |
ID (1) | ID21570A (en) |
PT (1) | PT929503E (en) |
WO (1) | WO1998014419A1 (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100413833C (en) * | 2004-04-16 | 2008-08-27 | 中国石油化工股份有限公司上海石油化工研究院 | Method for producing glycol by epoxy ethane hydration |
DE602004019076D1 (en) * | 2004-08-05 | 2009-03-05 | Saudi Basic Ind Corp | Process with a catalyst-coated heat exchanger |
CN100343212C (en) * | 2005-01-20 | 2007-10-17 | 中国寰球工程公司 | Evaporation system for producing ethylene glycol |
US7645906B2 (en) | 2007-03-27 | 2010-01-12 | Chevron Phillips Chemical Company Lp | Graded catalyst bed for methyl mercaptan synthesis |
US8053609B2 (en) * | 2007-10-15 | 2011-11-08 | Sd Lizenzverwertungsgesellschaft Mbh & Co. Kg | Solid catalyst useful for converting an alkylene oxide to an alkylene glycol |
BRPI0923998A2 (en) * | 2009-04-15 | 2016-01-26 | Invista Tech Sarl | method for treating perfluorosulfonic acid resin, perfluorosulfonic acid resin and process for making polyether glycol or copolyether glycol |
KR101307060B1 (en) * | 2011-10-17 | 2013-09-11 | 삼성토탈 주식회사 | Preparation method for diethyleneglycol by using multiple feeding of raw materials |
CN103709001B (en) * | 2012-10-08 | 2016-05-11 | 中国石油化工股份有限公司 | The method of Synthesis of Ethylene Glycol by Ethylene Oxide Hydration |
CN102875331B (en) * | 2012-10-28 | 2014-12-17 | 中国海洋大学 | Heat pump reaction rectification technology for preparing glycol through hydration of epoxy ethane |
CA3195635A1 (en) * | 2020-10-15 | 2022-04-21 | Sabic Global Technologies B.V. | System and process for producing glycols |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4165440A (en) * | 1976-10-06 | 1979-08-21 | Shell Oil Company | Catalytic hydration of ethylene oxide to ethylene glycol |
-
1997
- 1997-10-03 CN CN97199748A patent/CN1100742C/en not_active Expired - Fee Related
- 1997-10-03 KR KR1019990702932A patent/KR20000048902A/en not_active Application Discontinuation
- 1997-10-03 BR BR9712200-9A patent/BR9712200A/en not_active Application Discontinuation
- 1997-10-03 ES ES97909974T patent/ES2165589T3/en not_active Expired - Lifetime
- 1997-10-03 DE DE69707487T patent/DE69707487T2/en not_active Revoked
- 1997-10-03 JP JP10516921A patent/JP2001501624A/en active Pending
- 1997-10-03 ID IDW990154A patent/ID21570A/en unknown
- 1997-10-03 AT AT97909974T patent/ATE207050T1/en not_active IP Right Cessation
- 1997-10-03 PT PT97909974T patent/PT929503E/en unknown
- 1997-10-03 AU AU47458/97A patent/AU731453B2/en not_active Ceased
- 1997-10-03 WO PCT/US1997/017936 patent/WO1998014419A1/en not_active Application Discontinuation
- 1997-10-03 CA CA002268158A patent/CA2268158A1/en not_active Abandoned
- 1997-10-03 EP EP97909974A patent/EP0929503B1/en not_active Revoked
Also Published As
Publication number | Publication date |
---|---|
DE69707487D1 (en) | 2001-11-22 |
AU731453B2 (en) | 2001-03-29 |
ID21570A (en) | 1999-06-24 |
CN1100742C (en) | 2003-02-05 |
EP0929503B1 (en) | 2001-10-17 |
ATE207050T1 (en) | 2001-11-15 |
EP0929503A1 (en) | 1999-07-21 |
PT929503E (en) | 2002-02-28 |
DE69707487T2 (en) | 2002-04-11 |
AU4745897A (en) | 1998-04-24 |
WO1998014419A1 (en) | 1998-04-09 |
ES2165589T3 (en) | 2002-03-16 |
CN1237953A (en) | 1999-12-08 |
KR20000048902A (en) | 2000-07-25 |
CA2268158A1 (en) | 1998-04-09 |
JP2001501624A (en) | 2001-02-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BR9712200A (en) | Method for producing glycol | |
KR910007854A (en) | Method of producing monoepoxide | |
DE58902825D1 (en) | METHOD FOR PRODUCING POLYGLYCERINES. | |
Mimini et al. | Lignosulfonate-based polyurethane materials via cyclic carbonates: preparation and characterization | |
Pou et al. | Stereoselective Organocatalytic Approach to α, β‐Disubstituted‐β‐amino Acids: A Short Enantioselective Synthesis of Cispentacin | |
Proud et al. | Development of a protecting group for sulfate esters | |
Laprise et al. | Synthesis of a Renewable, Waste‐Derived Nonisocyanate Polyurethane from Fish Processing Discards and Cashew Nutshell‐Derived Amines | |
Tummatorn et al. | Convenient and direct azidation of sec-benzyl alcohols by trimethylsilyl azide with bismuth (III) triflate catalyst | |
Sîrbu et al. | Selectivity Control in Terpene Rearrangements: A Biomimetic Synthesis of the Halimanic Bicyclic Core | |
EP2321293B1 (en) | Process for producing epoxides | |
Jones et al. | One‐Pot Preparation of Enantiopure Fluorinated β‐Amino Acid Precursors | |
Hoff et al. | A Vicinal Diol Approach for the Total Synthesis of Molestin E, ent‐Sinulacembranolide A and ent‐Sinumaximol A | |
Di Bussolo et al. | d-Allal-and d-Galactal-Derived Vinyl N-Mesylaziridines: Regio-and Stereoselectivity in Addition Reactions of O-, C-, N-, and S-Nucleophiles | |
Maggi et al. | Reaction between epoxides and carbon disulfide under hydrotalcite catalysis: eco compatible synthesis of cyclic dithiocarbonates | |
Mulard et al. | Fluorination at position 6 of derivatives of methyl cx-D-galactopyranoside’ | |
RU2788109C1 (en) | Method for obtaining chlorohydrin compounds | |
RU2788008C1 (en) | Method for producing epoxy compounds from alkenes by chlorohydrine method | |
CN106630083B (en) | Harmless treatment method of epoxidized wastewater | |
US3988353A (en) | Preferential removal of metallic catalyst from epoxidation effluent | |
JPS56147764A (en) | Preparation of thioalkylene glycol | |
Luchetti et al. | Enantio-and Diastereodivergent Synthetic Route to Multifarious Cyclitols from D-Xylose via Ring-Closing Metathesis | |
KR20150069148A (en) | A Method and Apparatus for Treating Wastewater of Butene to Butadiene | |
ES2173567T3 (en) | PROCESS FOR THE MANUFACTURE OF HALOCARBONS. | |
Simao et al. | Controlled Garegg Conditions for Selective Iodination on Pyranose Templates | |
Sabitha et al. | Synthetic studies on callipeltin A: stereoselective synthesis of (2R, 3R, 4S)-3-hydroxy-2, 4, 6-trimethylheptanoic acid |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA10 | Dismissal: dismissal - article 33 of industrial property law | ||
B11Y | Definitive dismissal - extension of time limit for request of examination expired [chapter 11.1.1 patent gazette] |